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Mefloquine Hydrochloride

NDC 0555-0171 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerTeva Pharmaceuticals USA, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA076392
Dosage form / routeTABLET · ORAL
Active ingredientsMEFLOQUINE HYDROCHLORIDE (250 mg/1)
Marketing started20040106
Package count1

External sources

Source: openFDA. Public-domain (CC0).